From animal model to diabetic complications. Is there a therapy for diabetic polyneuropathy based on the pathogenesis of pain?

被引:0
|
作者
Treede, R. -D. [1 ]
机构
[1] Univ Heidelberg, Lehrstuhl Neurophysiol, Zentrum Biomed & Med Tech Mannheim CBTM, D-68167 Mannheim, Germany
来源
DIABETOLOGE | 2009年 / 5卷 / 05期
关键词
Neuropathic pain; Sensory loss; Hyperalgesia; Animal models; NEUROPATHIC PAIN; CLINICAL-TRIALS; EFFICACY; MECHANISMS; DESIPRAMINE; NEURONS; FIBERS; RAT;
D O I
10.1007/s11428-009-0392-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Approximately 1/3 of all diabetic patients develop a peripheral neuropathy, which often leads to chronic pain. First-line pharmacological treatments according to current guidelines (gabapentin, pregabalin, tricyclic antidepressants) were found empirically and not prospectively according to their mode of action. For 20 years it has been a postulate to develop treatment approaches according to the pathophysiological mechanisms of painful diabetic polyneuropathy. The lack of progress in this field is at least partially due to a mismatch between animal models and patient phenotypes. Animal models focus on increased responsiveness to mechanical stimuli, which is present in less than 20% of patients. Patients report mainly ongoing pain accompanied by sensory loss to touch, cold and pinprick.
引用
收藏
页码:344 / +
页数:5
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